Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02570 | A01 | 1166738 | G | A | upstream_gene_variant | MODIFIER | c.-4063G>A| |
S17 |
2 | BAA01g02570 | A01 | 1167101 | G | A | upstream_gene_variant | MODIFIER | c.-3700G>A| |
S149 |
3 | BAA01g02570 | A01 | 1168492 | G | A | upstream_gene_variant | MODIFIER | c.-2309G>A| |
S263 |
4 | BAA01g02570 | A01 | 1168607 | C | T | upstream_gene_variant | MODIFIER | c.-2194C>T| |
S270 |
5 | BAA01g02570 | A01 | 1168686 | C | T | upstream_gene_variant | MODIFIER | c.-2115C>T| |
S19 |
6 | BAA01g02570 | A01 | 1169165 | G | A | upstream_gene_variant | MODIFIER | c.-1636G>A| |
S178 |
7 | BAA01g02570 | A01 | 1169500 | G | A | upstream_gene_variant | MODIFIER | c.-1301G>A| |
S110 |
8 | BAA01g02570 | A01 | 1169991 | C | T | upstream_gene_variant | MODIFIER | c.-810C>T| |
S219 S72 |
9 | BAA01g02570 | A01 | 1170897 | G | A | missense_variant | MODERATE | c.97G>A|p.Asp33Asn |
S199 |
10 | BAA01g02570 | A01 | 1172813 | C | T | missense_variant | MODERATE | c.437C>T|p.Ala146Val |
S18 |
11 | BAA01g02570 | A01 | 1172842 | G | A | missense_variant | MODERATE | c.466G>A|p.Ala156Thr |
S115 |
12 | BAA01g02570 | A01 | 1174392 | C | T | missense_variant | MODERATE | c.1520C>T|p.Ser507Phe |
S35 |
13 | BAA01g02570 | A01 | 1174758 | C | T | missense_variant | MODERATE | c.1790C>T|p.Pro597Leu |
S223 |